Class II
Terminated
Moexipril Hydrochloride and Hydrocholorothiazide Tablets USP, 7.5 mg/12.5 mg, 100-count bottle, Rx only, Distributed By: TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, NDC 0093-5213-01.
- Company
- Teva Pharmaceuticals Usa
- Recall Initiated
- December 14, 2017
- Posted
- January 17, 2018
- Recall Number
- D-0208-2018
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 4,969 bottles
- Firm Location
- North Wales, PA, United States
Reason for Recall
Failed Impurities/Degradation Specifications: High out of specification test result for the Moexipril Diketopiperazine impurity was obtained during routine stability testing.
Distribution
Nationwide in the USA
Lot / Code Info
Lot # 30229439A, Exp 12/17
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